Statistical mechanics of dielectric fluids in electric fields: A mean‐field treatment

1981 ◽  
Vol 75 (7) ◽  
pp. 3559-3564 ◽  
Author(s):  
J. S. Ho/ye ◽  
G. Stell
2021 ◽  
Vol 48 (5) ◽  
Author(s):  
Ekhard K. H. Salje ◽  
Xiang Jiang

AbstractThe non-smooth, jerky movements of microstructures under external forcing in minerals are explained by avalanche theory in this review. External stress or internal deformations by impurities and electric fields modify microstructures by typical pattern formations. Very common are the collapse of holes, the movement of twin boundaries and the crushing of biominerals. These three cases are used to demonstrate that they follow very similar time dependences, as predicted by avalanche theories. The experimental observation method described in this review is the acoustic emission spectroscopy (AE) although other methods are referenced. The overarching properties in these studies is that the probability to observe an avalanche jerk J is a power law distributed P(J) ~ J−ε where ε is the energy exponent (in simple mean field theory: ε = 1.33 or ε = 1.66). This power law implies that the dynamic pattern formation covers a large range (several decades) of energies, lengths and times. Other scaling properties are briefly discussed. The generated patterns have high fractal dimensions and display great complexity.


Author(s):  
Andrea Rapisarda ◽  
Vito Latora

The Boltzmann-Gibbs formulation of equilibrium statistical mechanics depends crucially on the nature of the Hamiltonian of the JV-body system under study, but this fact is clearly stated only in the introductions of textbooks and, in general, it is very soon neglected. In particular, the very same basic postulate of equilibrium statistical mechanics, the famous Boltzmann principle S = k log W of the microcanonical ensemble, assumes that dynamics can be automatically an easily taken into account, although this is not always justified, as Einstein himself realized [20]. On the other hand, the Boltzmann-Gibbs canonical ensemble is valid only for sufficiently short-range interactions and does not necessarily apply, for example, to gravitational or unscreened Colombian fields for which the usually assumed entropy extensivity postulate is not valid [5]. In 1988, Constantino Tsallis proposed a generalized thermostatistics formalism based on a nonextensive entropic form [24]. Since then, this new theory has been encountering an increasing number of successful applications in different fields (for some recent examples see Abe and Suzuki [1], Baldovin and Robledo [4], Beck et al. [8], Kaniadakis et al. [12], Latora et al. [16], and Tsallis et al. [25]) and seems to be the best candidate for a generalized thermodynamic formalism which should be valid when nonextensivity, long-range correlations, and fractal structures in phase space cannot be neglected: in other words, when the dynamics play a nontrivial role [11] and fluctuations are quite large and non-Gaussian [6, 7, 8, 24, 26]. In this contribution we consider a nonextensive JV-body classical Hamiltonian system, with infinite range interaction, the so-called Hamiltonian mean field (HMF) model, which has been intensively studied in the last several years [3, 13, 14, 15, 17, 18, 19]. The out-of-equilibrium dynamics of the model exhibits a series of anomalies like negative specific heat, metastable states, vanishing Lyapunov exponents, and non-Gaussian velocity distributions. After a brief overview of these anomalies, we show how they can be interpreted in terms of nonextensive thermodynamics according to the present understanding.


1998 ◽  
Vol 53 (1-2) ◽  
pp. 17-26
Author(s):  
Mohamed Fahmy El-Sayed

Abstract A linear stability analysis of a novel electrohydrodynamic Kelvin-Helmholtz system consisting of the superposition of two uniformly rotating dielectric media is presented. The characteristic equation for such an arrangement is derived, which in turn yields a stability criterion for velocity differences of disturbances at a given rotation frequency. The conditions of stability for long and short wave perturbations are obtained, and their dependence on rotation, surface tension and applied electric field is discussed. Limiting cases for vanishing fluid velocities, rotation frequency, and applied electric field are also discussed. Under suitable limits, results of previous works are recovered. A detailed analysis for tangential and normal applied electric fields, in the presence and absence of surface charges, is carried out.


Author(s):  
Robert T. Balmer

Simultaneous energy transfer modes have been known to interact to produce unusual “coupled” effects. This coupling now has its theoretical basis in the concept of entropy production (or dissipation or irreversibility) central to nonequilibrium irreversible thermodynamics. Over the years, many examples of coupled phenomena have been identified and studied (thermoelectricity, electrokinetics, piezoelectricity, and so forth). Electrohydrodynamics (the effect of fluid motion on electric fields and the reverse effect of electric fields on fluid motion) can be explained as a thermodynamically coupled phenomenon characterized by the viscous and electrical properties of a fluid that contain mobile charges at the molecular (e.g., ions) or macroscopic (e.g., dust) levels. This is called the “viscoelectric” effect. In the first part of this paper we apply the concepts of irreversible thermodynamics to electrohydrodynamic systems to develop the relevant relationships. The second describes experiments carried out with a new type of Couette electrostatic generator. The resulting experimental data is then discussed in light of the coupled phenomenon relations previously developed.


Author(s):  
Ruy Batista Santiago Neto ◽  
Bernhard Lesche

The influence of electric fields on the velocity of the chemical reaction 4HF+SiO 2 →SiF 4 +2H 2 O in aqueous solution is investigated experimentally. The field strengths used were high enough to measure nonlinear effects. The results permit a critical analysis of a theoretical model known in literature. The basic idea of dipole orientation changing the rate of the primary step of the chemical reaction can explain the experimental data, but several important details of the original model had to be changed. The primary step involves two hydrogen fluoride (HF) molecules rather than one, and field screening by mobile ions has a significant influence causing nonlinear effects. The fact that field screening plays an important role implies that electric field-assisted HF etching of silica may by used as an instrument for measuring ion concentrations in highly concentrated electrolytes. The data measured may be well described by a theoretical model based on mean field approximations. The results give an insight into the structure of highly concentrated hydrofluoric acid and also permit a critical analysis of applications of the effect in measuring electric fields written in glass samples by electrothermal poling. The effect may also be used for shaping glass surfaces.


2001 ◽  
Vol 1 (1) ◽  
pp. 32
Author(s):  
P. M. Carrica ◽  
V. Masson

We present the results of an experimental study of the effects of externally imposed electric fields on boiling heat transfer and critical heat flux (CHF) in dielectric fluids. The study comprises the analysis of geometries that, under the effects of electric fields, cause the bubbles either to be pushed toward the heater or away from it. A local phase detection probe was used to measure the void fraction and the interfacial impact rate near the heater. It was found that the critical heat flux can be either augmented or reduced with the application of an electric field, depending on the direction of . In addition, the heat transfer can be slightly enhanced or degraded depending on the heat flux. The study of the two-phase flow in nucleate boiling, only for the case of favorable dielectrophoretic forces, reveals that the application of an electric field reduces the bubble detection time and increases the detachment frequency. It also shows that the two-phase flow characteristics of the second film boiling regime resemble more a nucleate boiling regime than a film boiling regime.


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